Optic AtrophyOptic Atrophy, Autosomal DominantOptic Atrophies, HereditaryAtrophyOptic NerveWolfram SyndromeOptic DiskGTP PhosphohydrolasesOptic Atrophy, Hereditary, LeberMuscular AtrophyOptic NeuritisHereditary Sensory and Motor NeuropathyOptic ChiasmRetinal Ganglion CellsPapilledemaPedigreeOptic Nerve InjuriesMuscular Atrophy, SpinalVision DisordersVisual AcuityDNA, MitochondrialBlindnessEye DiseasesOnchocerciasis, OcularRetinaMultiple System AtrophyOptic Neuropathy, IschemicOptic Lobe, NonmammalianGlutaratesOptic FlowGenes, RecessiveSyndromeMitochondrial DiseasesDiabetes InsipidusMitochondrial DynamicsMyoclonic Cerebellar DyssynergiaVision, LowMitochondrial ProteinsSpinal Muscular Atrophies of ChildhoodMutationMagnetic Resonance ImagingElectroretinographyOptics and PhotonicsMicrocephalyVisual FieldsCerebellar AtaxiaNerve FibersMutation, MissenseColor Vision DefectsFundus OculiOptic Nerve GliomaEvoked Potentials, VisualMitochondriaDNA Mutational AnalysisCodon, NonsenseOptic Nerve DiseasesOlivopontocerebellar AtrophiesConsanguinityGenetic HeterogeneityNADH DehydrogenaseLeigh DiseaseDeafnessVisual Field TestsGyrate AtrophyRetinal DiseasesGenes, DominantHearing Loss, SensorineuralDisease Models, AnimalChromosomes, Human, Pair 3PhenotypeGenetic LinkageIntellectual DisabilityNeurodegenerative DiseasesFounder EffectGeographic AtrophyMembrane ProteinsAbnormalities, Multiple